In This Issue
Editorials
- Where has all the white matter gone?Unraveling the mysteries of leukoencephalopathiesEdward M. Kaye, Hugo Moser
In Memoriam
Articles
- A prospective controlled study of cognitive function during an amateur boxing tournamentJ. Moriarity, A. Collie, D. Olson, J. Buchanan, P. Leary, M. McStephen, P. McCrory
- Severe hypomyelination associated with increased levels of N-acetylaspartylglutamate in CSFN. I. Wolf, M. A.A.P. Willemsen, U. F. Engelke, M. S. van der Knaap, P. J.W. Pouwels, I. Harting, J. Zschocke, E. A. Sistermans, D. Rating, R. A. Wevers
- The effect of genotype on the natural history of eIF2B-related leukodystrophiesA. Fogli, R. Schiffmann, E. Bertini, S. Ughetto, P. Combes, E. Eymard-Pierre, C. R. Kaneski, M. Pineda, M. Troncoso, G. Uziel, R. Surtees, D. Pugin, M. -P. Chaunu, D. Rodriguez, O. Boespflug-Tanguy
- Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathyS. Bohlega, S. N. Abu-Amero, S. M. Wakil, P. Carroll, R. Al-Amr, B. Lach, Y. Al-Sayed, E. J. Cupler, B. F. Meyer
- Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second geneN. Bissar-Tadmouri, E. Nelis, S. Züchner, Y. Parman, F. Deymeer, P. Serdaroglu, P. De Jonghe, V. Van Gerwen, V. Timmerman, J. M. Schröder, E. Battaloglu
- B- and T-cell markers in opsoclonus–myoclonus syndromeImmunophenotyping of CSF lymphocytesM. R. Pranzatelli, A. L. Travelstead, E. D. Tate, T. J. Allison, E. J. Moticka, D. N. Franz, M. A. Nigro, J. T. Parke, D. A. Stumpf, S. J. Verhulst
- Measuring progression of cerebral white matter lesions on MRIVisual rating and volumetricsN. D. Prins, E. C.W. van Straaten, E. J. van Dijk, M. Simoni, R. A. van Schijndel, H. A. Vrooman, P. J. Koudstaal, P. Scheltens, M. M.B. Breteler, F. Barkhof
- Analgesic overuse among subjects with headache, neck, and low-back painJ. -A. Zwart, G. Dyb, K. Hagen, S. Svebak, L. J. Stovner, J. Holmen
- Risk factors for postherpetic neuralgia in patients with herpes zosterBeth F. Jung, Robert W. Johnson, David R.J. Griffin, Robert H. Dworkin
- Randomized, placebo-controlled trial of rofecoxib in the acute treatment of migraineS. Silberstein, S. Tepper, J. Brandes, M. Diamond, J. Goldstein, P. Winner, S. Venkatraman, F. Vrijens, W. Malbecq, C. Lines, W. H. Visser, S. Reines, E. Yuen
- Stroke patterns, etiology, and prognosis in patients with diabetes mellitusTh. Karapanayiotides, B. Piechowski-Jozwiak, G. van Melle, J. Bogousslavsky, G. Devuyst
- Decreased transferrin receptor expression by neuromelanin cells in restless legs syndromeJ. R. Connor, X. S. Wang, S. M. Patton, S. L. Menzies, J. C. Troncoso, C. J. Earley, R. P. Allen
- Striatal dopamine transporter in dementia with Lewy bodies and Parkinson diseaseA comparisonZ. Walker, D. C. Costa, R. W.H. Walker, L. Lee, G. Livingston, E. Jaros, R. Perry, I. McKeith, C. L.E. Katona
- Dietary fat intake and 6-year cognitive change in an older biracial community populationM. C. Morris, D. A. Evans, J. L. Bienias, C. C. Tangney, R. S. Wilson
- Amyloid β(1–42) and phosphorylated tau in CSF as markers for early-onset Alzheimer diseaseN. S.M. Schoonenboom, Y. A.L. Pijnenburg, C. Mulder, S. M. Rosso, E. -J. Van Elk, G. J. Van Kamp, J. C. Van Swieten, Ph. Scheltens
- Neuroimaging findings in scleroderma en coup de sabreS. Appenzeller, M. A. Montenegro, S. San Juan Dertkigil, P. D. Sampaio-Barros, J. F. Marques-Neto, A. M. Samara, F. Andermann, F. Cendes
Special Article
- Assessment: Transcranial Doppler ultrasonography: [RETIRED]Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology*M. A. Sloan, A. V. Alexandrov, C. H. Tegeler, M. P. Spencer, L. R. Caplan, E. Feldmann, L. R. Wechsler, D. W. Newell, C. R. Gomez, V. L. Babikian, D. Lefkowitz, R. S. Goldman, C. Armon, C. Y. Hsu, D. S. Goodin
Views & Reviews
- Clinical and histologic findings in autosomal centronuclear myopathyP.-Y. Jeannet, G. Bassez, B. Eymard, P. Laforêt, J. A. Urtizberea, A. Rouche, P. Guicheney, M. Fardeau, N. B. Romero
Clinical/Scientific Notes
- State-specific projections through 2025 of Alzheimer disease prevalenceL. E. Hebert, P. A. Scherr, J. L. Bienias, D. A. Bennett, D. A. Evans
- Prolonged interval between vertebral artery dissection and ischemic strokeFozia S. Nazir, Keith W. Muir
- Carotid artery dissection after prolonged head tilting while holding a newborn baby to sleepOi-yan Yannie Soo, Yu Leung Chan, Ka Sing Wong
- CSF tau and Aβ42 are not useful in the diagnosis of frontotemporal lobar degenerationY. A.L. Pijnenburg, N. S.M. Schoonenboom, S. M. Rosso, C. Mulder, G. J. Van Kamp, J. C. Van Swieten, P. Scheltens
NeuroImages
- Brachiocephalic trunk stenosis mimicking giant cell arteritisAshok Srinivasan, Peter Stys, Cheemun Lum, Mayank Goyal
Correspondence
- Clinical characteristics of responders to interferon therapy for relapsing MSPablo Villoslada, Jorge R. Oksenberg, Jordi Rio, Xavier Montalban
- Bilateral motor cortex disinhibition in complex regional pain syndrome (CRPS) type I of the handPhillip Krause, S. Foerderreuther, A. Straube
- Myelopathy due to copper deficiencyCalin I. Prodan, Neil R. Holland, Peggy J. Wisdom, Sylvia S. Bottomley
Departments
Historical Neurology
- The birth of nerve agent warfareLessons from Syed Abbas ForoutanCol. Jonathan Newmark
Brief Communications
- Arg113His mutation in eIF2Bε as cause of leukoencephalopathy in adultsM. S. van der Knaap, P. A.J. Leegwater, C. G.M. van Berkel, C. Brenner, E. Storey, M. Di Rocco, F. Salvi, J. C. Pronk
- Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B5H. Ohtake, T. Shimohata, K. Terajima, T. Kimura, R. Jo, R. Kaseda, O. Iizuka, M. Takano, Y. Akaiwa, H. Goto, H. Kobayashi, T. Sugai, T. Muratake, T. Hosoki, T. Shioiri, K. Okamoto, O. Onodera, K. Tanaka, T. Someya, T. Nakada, S. Tsuji
- Neurologic manifestations of Kanzaki diseaseF. Umehara, K. Matsumuro, Y. Kurono, K. Arimura, M. Osame, T. Kanzaki
- Distal myopathy with rimmed vacuoles (DMRV)New GNE mutations and splice variantH. Tomimitsu, J. Shimizu, K. Ishikawa, N. Ohkoshi, I. Kanazawa, H. Mizusawa
- HFE mutations are not strongly associated with sporadic ALSA. A. Yen, E. P. Simpson, J. S. Henkel, D. R. Beers, S. H. Appel
- Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephalyU. Aguglia, A. Gambardella, G. J. Breedveld, R. L. Oliveri, E. Le Piane, D. Messina, A. Quattrone, P. Heutink
- Genes influencing Parkinson disease onsetReplication of PARK3 and identification of novel lociN. Pankratz, S. K. Uniacke, C. A. Halter, A. Rudolph, C. W. Shults, P. M. Conneally, T. Foroud, W. C. Nichols, the Parkinson Study Group
- Autosomal dominant parkinsonism associated with variable synuclein and tau pathologyZ. K. Wszolek, R. F. Pfeiffer, Y. Tsuboi, R. J. Uitti, R. D. McComb, A. J. Stoessl, A. J. Strongosky, A. Zimprich, B. Müller-Myhsok, M. J. Farrer, T. Gasser, D. B. Calne, D. W. Dickson
- Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridineM. Strupp, R. Kalla, M. Dichgans, T. Freilinger, S. Glasauer, T. Brandt
- Ropinirole in Gilles de la Tourette syndromeMarietta H. Anca, Nir Giladi, Amos D. Korczyn
- EEG abnormalities in frontotemporal lobar degenerationD. Chan, R. J. Walters, E. L. Sampson, J. M. Schott, S. J. Smith, M. N. Rossor
- Alzheimer disease risk associated with APOE4 is modified by STH gene polymorphismD. Seripa, M. G. Matera, R. P. D’Andrea, C. Gravina, C. Masullo, A. Daniele, A. Bizzarro, M. Rinaldi, P. Antuono, D. R. Wekstein, G. Dal Forno, V. M. Fazio
- Serum S100β increases in marathon runners reflect extracranial release rather than glial damageM. Hasselblatt, F. C. Mooren, N. von Ahsen, K. Keyvani, A. Fromme, K. Schwarze-Eicker, V. Senner, W. Paulus
- Language dysfunction after frontal lobe partial seizuresHadassa Goldberg-Stern, Nathan Gadoth, William Cahill, Michael Privitera
- Clinical profile and course of cognitively normal patients evaluated in memory disorders clinicsEmily R. Edwards, Karla Lindquist, Kristine Yaffe
Nisus: Neurology and the Humanities
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